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01 1Agno Pharma Jiangsu

02 1F.I.S. Fabbrica Italiana Sintetici S.P.A.

03 1Olon SpA

04 1Spectrum Laboratory Products, Inc.

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PharmaCompass

01

RDD 2025
Not Confirmed
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RDD 2025
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SULINDAC

NDC Package Code : 57821-015

Start Marketing Date : 2024-12-04

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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02

RDD 2025
Not Confirmed
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RDD 2025
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SULINDAC

NDC Package Code : 52133-0007

Start Marketing Date : 1982-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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03

RDD 2025
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04

RDD 2025
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RDD 2025
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SULINDAC

NDC Package Code : 49452-7583

Start Marketing Date : 1996-04-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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Looking for 38194-50-2 / Sulindac API manufacturers, exporters & distributors?

Sulindac manufacturers, exporters & distributors 1

15

PharmaCompass offers a list of Sulindac API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Sulindac manufacturer or Sulindac supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulindac manufacturer or Sulindac supplier.

PharmaCompass also assists you with knowing the Sulindac API Price utilized in the formulation of products. Sulindac API Price is not always fixed or binding as the Sulindac Price is obtained through a variety of data sources. The Sulindac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Sulindac

Synonyms

Clinoril, 38194-50-2, Arthrocine, Artribid, Sulindaco, Sulindacum

Cas Number

38194-50-2

Unique Ingredient Identifier (UNII)

184SNS8VUH

About Sulindac

A sulfinylindene derivative prodrug whose sulfinyl moiety is converted in vivo to an active NSAID analgesic. Specifically, the prodrug is converted by liver enzymes to a sulfide which is excreted in the bile and then reabsorbed from the intestine. This helps to maintain constant blood levels with reduced gastrointestinal side effects.

Imbaral Manufacturers

A Imbaral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imbaral, including repackagers and relabelers. The FDA regulates Imbaral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imbaral API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Imbaral manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Imbaral Suppliers

A Imbaral supplier is an individual or a company that provides Imbaral active pharmaceutical ingredient (API) or Imbaral finished formulations upon request. The Imbaral suppliers may include Imbaral API manufacturers, exporters, distributors and traders.

click here to find a list of Imbaral suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Imbaral NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Imbaral as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Imbaral API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Imbaral as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Imbaral and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Imbaral NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Imbaral suppliers with NDC on PharmaCompass.

Imbaral Manufacturers | Traders | Suppliers

Imbaral Manufacturers, Traders, Suppliers 1
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We have 4 companies offering Imbaral

Get in contact with the supplier of your choice:

  1. Agno Pharma
  2. F.I.S. Fabbrica Italiana Sintetici
  3. Olon S.p.A
  4. Spectrum Chemical
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.